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J Med Chem ; 50(24): 6284-8, 2007 Nov 29.
Article in English | MEDLINE | ID: mdl-17973470

ABSTRACT

Conjugates of curcumin to two differently sized poly(ethylene glycol) molecules were synthesized in an attempt to overcome the low aqueous solubility of this natural product with cytotoxic activity against some human cancer cell lines. The soluble conjugates exhibited enhanced cytotoxicity as compared to that of the parent drug. Synthesis, analyses of the rate of drug release, and cytotoxicity studies are herein reported. The water-soluble conjugates may provide information useful for the development of injectable curcumin conjugates.


Subject(s)
Antineoplastic Agents/chemical synthesis , Curcumin/chemistry , Polyethylene Glycols/chemistry , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Cell Line, Tumor , Drug Design , Drug Screening Assays, Antitumor , Humans , Solubility , Structure-Activity Relationship , Water
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